For healthcare professionals only.
EU Summary of Product CharacteristicsA NEW IMNOVID® (pomalidomide) TRIPLET
IMNOVID with bortezomib
and dexamethasone, PVd
NOW APPROVED IN THE EU
for RRMM as early as first relapse, post-REVLIMID®
(lenalidomide)1
Indication
IMNOVID in combination with bortezomib and
dexamethasone is indicated in the treatment of adult
patients with multiple myeloma who have received at
least one prior treatment regimen including lenalidomide.
RRMM=relapsed/refractory multiple myeloma.
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References: 1. IMNOVID [Summary of Product Characteristics]. Utrecht, Netherlands, Celgene Europe B.V.; 2019. 2. Dimopoulos M, et al. ASH 2018. Abstract no. 3278.
PVd=IMNOVID+bortezomib+ dexamethasone.
03/19 INT-POMA190004
PVd is the first and only triplet specifically
proven in a 100% REVLIMID-exposed RRMM
population as early as first relapse.2